Process for preparing beta-lactones



Patented Sept. 28, 1948 UNITED STATES PATENT or FICE 2,450,131 I 'raooliss'roit PREPARING-amorous -'Hugh -J. flagemeyer, J r., Kingsport, Tenn, as-

;signor'to Eastman Kodak Company, Rochester,

N. Y., a corporation of New Jersey No-D'raiwing. Application December 17, 1946, Serial No. 716,873

is-clams. (c1. 260-344) 0.1 g I "This invention relates to a processforpreparingFB-lactones'i. e. lactones of p-hydroxy-earboxylic =acids, from ketenes and aldehydes, ke-

tones;diketones and Kate carboxylic esters.

- Sisaudinger first showed that aketo-ketenes-such as=diphenyl -ketene,-added to aldehydesor ketones -to= give p-iactones. 384, 38-135-(l911)-and -Anni380;=243 (I911) staudingeralsoshowed'the additions of d-iphenyl tones, and isolateddiolefins from" the reaction -mixture. 401, 263 (-1913);

Aldo ketenes; on the other hand, are relatively unstable ascompared" withketo-ketenes and di- --nierize rapidly, under ordinary conditions of temperature and-pressure. In theabsence-of a cata- '-lyst, 'aldo ketenesrlo not condense withcarbonyl --compoun'ds, but form the dimer instead. With aldehydes, theketene' dimers react to form unsaturated ketones. See Boese, United States-Patent 2,108,427; dated February 15, 1938.

Kung in United States Patent 2,356,459; dated August 22, -l944,-has shown that ketene (CRE -C tones; in 'tl'ie'pr'esence' of Frieda-Crafts type "or 1 catalysts.

I have new found-that," in the presence'of an ester of "or-tho ormetaphosphoric acid, ketenes (both aldo' and keto ketenes) react wlth carhonyl compounds selected from the group consisting of ketene to unsaturated ke- "enceof at least one-ester ethyl groups, 1. e. alkyl groups of selected from thegroup consisting of esters of orthophosphoric acid-and esters of metaphosphoric acid.

*The ketenes which are advantageously employed lu -practicing my invention can be represented by the following general formula:

x 'whe'rein'R and R1 each represnta hydrogen atom,an'alkyl*group '(i. e. especially methyl and the formula CnH'am whereinm represents 'a positive integer phenyl group,

of from 1 to 2) or an aryl group (especially a p i; e. a Carla-group). "Although-my invention-"is directed primarily toa process involving =ketene (CH2=C=O) any aldo ketone' or anyke'to ketorie can be" employed. Typical aldo *al'dehydes, ketones, diketones 'and'ketocarboiiylie esters to give 13-lactones,- 'eventhough keten'eand keton'esi'react int'he presence of ortho' phosphoric acid itself togive' enol acetates. See Gwyfin and Degering United States'-Patnt'2,383;965, dated -September "l'hacatalysts "of my process are superior to'the IE'rledel-Crafts type of catalyst, in that separation "ofthe fr-lactone' from the reaction mixture may Ice-accomplished in the-presence oi the catalyst. This is-important because of the instability of the'p-laetones which inthe caseof the'Frledel- Crafts type of catalyst necessitate the removalor neutralizat-ionof the catalyst-before separation of the p-laotone-from the reactionmixture can be satisfactorilyacoomplished.

It is, accordingly, an object ofmy invention to providej animproved process for preparing S-lactones. Other objects will become apparent-hereinafter. a

In-accordance with my invention, I prepare 5- lactones 'by'reacting a ketene (either an aldo kete'n'e'or a lieto ketene) with an aldehyde, a ketone, a diketone oraketo carboxylic ester, in themesiietones' include ketene, methyl ketene, ethyl-ketene;etc. Typicalketo'ketones include dimethyl ketene, diethyl ketene, diphenyl ketenej methyl 'phenyl ketenejetc.

'The 'al-dehydes which V are advantageously enlployed'in --practiclng my invention can be represented by thefollowing general formula:

, wherein R2 represents an alkylgroup (especially methyL-ethyl, isepropyl, n-propyL- n-butyl, isobutyl, secondary butyl and tertiary butyl groups, 1. e. an alkyl group of the formula CnH21L+1 wherein n represents a positive integer-of from 1 to 4), an aralkyl group (especially benzyl or p-phenylethyl), and an aryl group (especially a monocyclic 'aryl group of the benzneseriesia g. phe'nyl, m-

is especially useful for the preparation of B-lactones from aldeh'ydes-of the-above general f ormula' wherein-R2 represents a hydrogen atom ora 'm'ethyl'group.

The 'ketones which are advantageously'employed in practiclng' my invention canbe represented by the following general formula:

wherein Bs represents an alkyl--group (especially methyl, ethyl, isopropyl, n-propyl, n-butyl, isobutyl secondary butyl and tertiary butyl groups,

i; e; an alkyl 'roiipof the. formula CnH2n+1 wherein n represents a-positive integer of from 1 to 4),

of the benzene series, e. g. phenyl, m-tolyl and ptolyl), or an aralkyl group (especially benzyl and B-phenylethyl), and R4 represents an alkyl group (especially methyl and ethyl groups) an aryl group (especially a monocyclic aryl group of the benzene series, e. g. phenyl, m-tolyl and p-tolyl) or an aralkyl group (especially benzyl and 3- phenylethyl). My new process is especially usein] for the preparation of fi-lactones from the above-formulated ketones wherein R4 represents a methyl group.

The diketones which are advantageously employed in practicing my invention can be represented by the following general formula:

R5( (C 9)m-1 5 wherein R5 and Re each represent an alkyl group (especially a methyl, an ethyl or an n-propyl group) and 172 represents a positive integer of from 1 to 3.

The keto carboxylic esters which are advantageously employed in practicing my invention can be represented by the following general formula:

wherein R7 represents an alkyl group (especially methyl and ethyl groups), R8 represents an alkyl group (especially methyl, ethyl, isopropyl, npropyl, n-butyl, isobutyl and secondary butyl groups) and m represents a positive integer of from 1 to 3.

Typical of the aldehydes, ketones, diketones and keto carboxylic esters are: formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, isobutyraldehyde, phenylacetaldehyde, benzaldehyde, p-methylbenzaldehyde, crotonaldehyde, furfuraldehyde, acetone, ethyl methyl ketone, methyl n-propyl ketone, methyl isopropyl ketone, methyl n-butyl ketone, methyl isobutyl ketone, diethyl ketone, methyl isopropenyl ketone, acetophenone, methyl benzyl ketone, p-methylacetophenone, diacetyl, dipropionyl, di-n-butyryl, diisobutyryl, acetyl acetone, hexanedione-2,4, methyl pyruvate, ethyl pyruvate, methyl acetoacetate, ethyl acetoacetate, n-propyl acetoacetate, n-butyl acetoacetate, ethyl levulinate, etc.

The catalysts which are-advantageously employed in practicing my invention can be represented by the following general formulas:

and R4-P 0:

wherein R1, R2, R3 and R4 each represents a member selectedfrom the group consisting of an alkyl group (i. e. an alcohol radical) especially a primary alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 4 phate, diethyl orthophosphate, diphenyl orthophosphate, triphenyl orthophosphate, tIl-anaphthyl orthophosphate, tri-fi-naphthyl 0rthophosphate, ethyl metaphosphate, n-propyl metaphosphate, n-butyl metaphosphate, phenyl metaphosphate, n-amylmetaphosphate, etc.

The quantity of catalyst employed can be varied and optimum concentrations are usually a function of the reactants employed. Ordinarily a concentration of catalyst equal to from about 0.1 to about 3% by weight of the total (all reactants plus solvent, if any) reaction mixture is advantageously employed. Higher concentrations of catalyst can be used, although ordinarily there is no advantage in doing so.

Where the carbonyl compound employed is an aldehyde, it is advantageous ordinarily to add the ketene and the aldehyde simultaneously and in equimolecular proportions to the catalyst or to a medium containing the catalyst. Where the carbonyl compound employed is a ketone, diketone or a keto carboxylic ester, the ketene is ordinarily advantageously added to the ketone or keto carboxylic ester containing the catalyst.

Advantageously my new process is carried out in a solvent for the reactants, i. e. an organic liquid which dissolves both the ketene and the aldehyde, ketone, diketone or keto carboxylic ester, and which is relatively inert to the reactants. Suitable solvents include the dialkyl ethers which are liquid at 10 C.,'e. g. diethyl ether, ethyl isopropyl ether, diisopropyl ether, ethyl n-butyl ether, methyl n-propyl ether, etc., cyclic ethers which are liquid at 10 0., e. g. 1,4-dioxane, chlorinated hydrocarbons which are liquid at 10 C., e. g. chloroform, carbon tetrachloride, ethylidene dichloride, ethylene dichloride, etc., hydrocarbons which are liquid at 10 C., e. g. benzene, toluene, etc.

In the case of the lower aldehydes, such as formaldehyde and acetaldehyde, ketones which are liquid at 10 C. can be employed as solvents because formaldehyde and acetaldehyde react with the ketenes much faster than do the ketones to give p-lactones in accordance with my process. Acetone and methyl ethyl ketone are advantageously employed as solvents when formaldehyde or acetaldehyde is employed.

The, fl-laotones, themselves, are excellent solvents ln which to carr out my new process and are the preferred solvents.

The process of my invention is advantageously carried out at temperatures below 50 C. Ordinarily temperatures between about 10 and about 20 C. are preferred, although temperatures as low as -50 C. can be employed.

The process of my invention can be carried out batchwise or continuously (e. g. in the continuous manner described in the copending application of Hugh J. Hagemeyer, Jr., and Delmer C. Cooper, Serial No. 660,286, filed April 6, 1946) Where ketene (CH2=C=O) is prepared by the catalytic pyrolysis of acetic acid at reduced pressures, it is advantageous to carry out the process at reduced pressure in a scrubber-type reactor, e. g. ketene and formaldehyde can be reacted at reduced pressure in a scrubber-type reactor (in the manner described in the copending application of Herbert G. Stone, Serial No. 660,285, filed April 6, 1946), using ,c-propionolactone as a solvent and boric acid as a catalyst.

Many of the ,B-lactones can be distilled from the, reaction mixtures under reduced pressures. However, many of the fl-lactones derived from aldehydes and ketones containing olefinic or acetylenic -bonds (e. :g. crotonaldehyde, fmethyl isopro'penyl "ketene, iurfuraldehyde, etc.) and many of t'h-e B-lactones derived from .k6t0 carboxylic esters and diketones cannot-be distilled, even under reducedpressure; without undergoing decarboxylation, i. e. loss of carbon dioxide, to give unsaturated compounds. Even the lower molecular weight fl-lactones derived from lower molecular weight aldehydes and ketones, e. g. formaldehyde, acetaldehyde, acetone and ethyl methyl .ketone, have a tendency to polymerize when heated. With these lower molecular weight p-fl'actones, it is advantageous to flash distill (ie. fdistill rapidly under a low vacuum, the pump :producingthe vacuum having a capacity-greater than:the-wolurne of vapor in the still) the reaction mixture and then to purify further theelactone by fractional redi'sti-llation under reduced -press'ure.

:The following .exam'ples'wlll serve to illustrate further" the mannerof practicing my invention.

Example 1.-Lactone ofp-hydroxypmpionic acid 4 (fir-PTOIJiOTLOZCLCtOflB) 50 g. of triethyl phosphate were added to 6 liters of methyl ethyl ketone. The solution, under reduced pressure, was charged to a stainless steel scrubber-reactor exactly like the scrubberreactor described in the copending application of Herbert G. Stone, Serial No. 660,285, filed April 6,1946. The catalyst solution was charged into the top of the scrubber-reactor where it fell on a dispersion plate, through the openings of which it trickled down onto the berl saddle packing in the scrubber-reactor. The catalyst solution was circulated'from the bottom to the top of the reactor through a conduit by means of a pump. Ketene (CHZZCFO) and formaldehyde ('7 ggper minuteand 5g. per minute respectively) were mixed immediately before entering the scrubber through anozzle placed below the screen supporting the packing near the bottom of the y *scrubiber. The scrubber and circulating lines were cooled to 0 C. The pressure drop across "the'scrubber was maintained at 30 to 40 mm. of

"Hg and the pressure at the top of the scrubber Was'40 mm. of Hg. The reaction between the formaldehyde and ketene began immediately upon contact with the recirculating stream oi catalyst solution and continued as the ketene "and formaldehyde rose to the top of the scrubberreact'or. The {3-propionolactone which was formed descended and entered a tank at the bottom of the scrubber-reactor from which it was continually removed. 3162 g. of formaldehyde and 4500 g. of ketene were bled into the scrubber during a 36 hour run. At the end of this time, distillation of the composite take-offs gave a 55%.yield-of S-propionolactone boiling at 82 to 83 C. at 100 mm. of-Hg pressrure'ND 1.4129.

Example 2.Lactone of c-hydrorybatyric acid (p-butyrolactone) CHa-CHCHr-?=O troduced; while cooling the reaction mixture at ing the reaction mixture 6 10' to 10 LC. 1 Distillation of the resulting: mixture gave 34 g. of fi-butyrolactone boiling at54 C. at

10 mm. of Hg pressure.

Example 3.--Lactone of ;8hydroxy-c-methylbatyric acid (18-methyl.-c-batyrolactone) 2 g. of ethyl metaphosphate were added to 250 ml. of acetone. Ketene (CI-I.z=C=O) 'was led into themixture through a hollow shaft high speed stirrer while the solution was held at 20 C. 42 .g. of ketene were introduced over a period of 2 hours. Upon distillation of the vreaction-1111xture, 26 g. of c-mothyl-c-butyrolactone, boiling at 55C. at 10 mm. of Hg, were obtained.

Example 4.-Lactone of p-carbethoxymethyl-phydroxybutyric acid oer-00001115 CHr- CH --C=O 3-methyl-3-butenoic acid-boiling at 545 C. at'

20 mm. of Hg pressure, were obtained. This ester has the following formula:

In the foregoing example ethyl acetoacetate can be replaced with methyl acetoacetate, n-propyl acetoacetate or n-butylacetoacetate for example.

Example 5.-Lact0ne of p acetylmeth'yl-c-hyd'rorypropiom'c acid Ketene (CH2=C=O) was passed in 300 cc. of an acetylacetone solution containing 1% by weight of a mixture consisting of approximately equal parts 'by weight of ethyl me'taphosphate and tetraethyl py-rophospha-te. In an eight hour run, about 84 g. of ketene were introduced, while coolat 0 to 10 C. The resulting reaction mixture contained a large proportion of the above-formulated lactone and some of the dilactone of the-following formula:

boiling 'at'88' C. at 735mm. oi-Hg pressure and 41 g. of Z-methyI-penten-l-one-el of the following formula:

boiling at 127 C. at 735 mm. of Hg pressure were obtained.

In the manner illustrated in the foregoing examples the other fi-lactones can be prepared. Thus in Example 3, if 3.5 gram-moles of propiorraldehyde are employed instead of 250 ml. of acetone at 10 0., B-valerolactone of the formula:

can be produced; 3.5 gram-moles of n-butyraldehyde at 10 C. gives fi-caprolactone of the formula:

etc.

What I claim as my invention and desire to be secured by Letters Patent of the United States is:

1. A process for preparing a fi-lactone comprising reacting a ketene selected from the ketenes represented by the following general formula:

o=o=o R1 wherein R and R1 each represents a member se lected from the group consisting of a hydrogen atom, a methyl group, an ethyl group and a phenyl (CsH5) group, with a carbonyl compound selected from the group represented by the following four general formulas:

R2 Rt wherein R2 represents a member selected from the group consisting of a hydrogen atom, an alkyl group of the formula CnH2n+l wherein n represents a positive integer of from 1 to 4, a benzyl group, a [i-phenylethyl group and a phenyl (CsH--) group, R3 represents a member selected from the group consisting of an alkyl group of the formula CHI-Ian wherein n represents a positive integer of from 1 to 4, R5 and Re each represents an alkyl group of the formula CnHZn-H wherein n represents a positive integer of from 1 to 3, R7 represents an alkyl group selected from the group consisting of methyl and ethyl groups, and R8 represents a member selected from the group consisting of primary and secondary alkyl groups of the formula CnH2n+l wherein n represents a positive integer of from 1 to 4 and m represents a positive integer of from 1 to 3, in the presence of at least one catalyst selected from the group consisting of the esters represented by the following general formulas:

0R1 O=POR2 0R3 wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnHZn-i-l wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, and R2, Rsand R4 each represents a member selected from the group consisting of a primary alkyl group of the formula CnH2n+l wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms at a temperature below 50 C.

2. A process for preparing a fl-lactone comprising reacting lzetene (CH2=C=O) with a carbonyl compound selected from the group represented by the following four general formulas:

wherein R2 represents a member selected from the group consisting of a hydrogen atom, an alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 4, a benzyl group, a fi-phenyletnyl group and a phenyl (CeH5-) group, R3 represents a member selected from the group consisting of an alkyl group of the formula CnHZn-H wherein n represents a positive integer of from 1 to 4, R5 and Rs each represents an alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 3, R7 represents an alkyl group selected from the group consisting of methyl and ethyl groups, and R8 represents a member selected from the group consisting of primary and secondary alkyl groups of the formula CnH2n+l wherein n represents a positive integer of from 1 to 4, and m represents a positive integer of from 1 to 3, in the presence of at least one catalyst selected from the group consisting of the esters'represented by the followin general formulas:

wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnH2n-H Where in n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, and R2, R3 and R4 each represents a member selected from the group consisting of a primary alkyl group of the formula CnH2n+l wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, at a temperature below 50 C.

3. A process for preparing a fi-lactone comprising reacting ketene (CH2=C=O) with a carbonyl compound selected from the group saro represented by:- the following; four general- I ll n-t(om)mt1m R1(J(QH 2)mOO=-Rs wherein R2 represents a-member selected frorn the group consisting'of ahydrogenatom, an alkyl group of theformula CnHZn-FL wherein. n-represents a positive integer offrom -1- -to 4,;a benzyl' group, a fi-phenylethyl group -and aflphenyl (CeH5-'-)- group, R3- represents almemberwsele'cted from the group, consisting. of an alkyl group of the formula CnH2n+l wherein: representa positive integer of from; 1 to 4, Raand Re each represents an alkyl group of the formula Cullen.-

alkyl groups of the formula Cnw'm-r wherein nrepresents a positive integeriof from 12 to 4, and m represents a positive integer of from 1 to 3, in the/presence of at least one catalyst selectedfrom" the group consisting of the esters represented by the following'general formulas:

OR! g O='P--OR2 and Ki -B08 wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to carbon atoms, and R2, R3 and R4 each represents a member selected from the group consisting of a primary alkyl group of the formula cnHzn-l-l wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, at a temperature of from about 10 to about 20 C.

4. A process for preparin fl-propionolactone comprising reacting ketene (CH2=C=O) with formaldehyde, in the presence of from about 0.1 to about 3% by weight of the material in the reaction mixture of at least one catalyst selected from the group represented by the following general formulas:

wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, and R2, R3 and R4 each represents a member selected from the group consisting of a primary alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, at a temperature of from about 10 to about 20 C.

5. A process for preparing fi-propionolactone comprising reacting ketene (CH2=C=0) with formaldehyde, in the presence of from about 0.1 to about 3% of the weight of the material in the reaction mixture of triethyl orthophosphate, at a temperature below 50 C.

and R4-P 0s 6; A process for preparing ,B-propionolactone comprising. reactingketene (CH2=C=O) with formaldehyde; inthe=presence of from about 0.1 to about 3% of the weight of'the material in the reactionmixture of triethyl orthophosphate, at a temperature'of from about 10 to about 20 C.

'7'. A processfor preparing fi-propionolactone comprising; adding ketene (CH2==C=O)' and formaldehyde in about equimolecular proportions to a solution of at least one catalyst selected from those represented by the following formulas:

and. R1"? 03 wherein Ri represents a -member selected from the 'group' consisting of'a hydrogen atom, a primary alkyil group of the formula CnH2n+1 wherein nrepresents a positive integer of from 1 to 5, and an-aryl hydrocarbon radical containing from 6 tol ll c'arbon atoms,-'and R2, R3 and R4 each represents amemner I selected from the group consisting of 'a-p'riniary alkyl group of the formula CnH'zHr wherein n' represents apositive integer of from 1 to 5,- and 'an arylhydrocarbon radical containiri'g'from-6*to10 carbon atoms",- in a sol. vent selected from the group consisting of acetone, ethyl methyl'ket'one and ,B-propionolactone,

at a temperature below 5001, the concentration of the catalystbeing e'quivalent to from about 0.1 toabout 3% by weight-of the materials -in-the reaction mixture;

A process forpreparing 3-'propionolactone comprising adding ketene (CH2=C=O) and formaldehyde in about equimolecular proportions to a solution of at least one catalyst selected from those represented by the following formulas:

and R4P 03 wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnH2n+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, and R2, R3 and R4 each represents a member selected from the group consisting of a primary alkyl group of the formula CnHzn+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, in a solvent selected from the group consisting of acetone, ethyl methyl ketone and p-propionolactone, at a temperature of from about 10 to about 20 C., the concentration of the catalyst being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture.

9. A process for preparing ,B-propionolactone comprising adding ketene (CH2=C=O) and formaldehyde in about equimolecular proportions to a solution of triethyl orthophosphate in a solvent selected from the group consisting of acetone, methyl ethyl ketone and s-propionolactone, the concentration of the triethyl orthophosphate being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture, at a temperature below 50 C.

10. A'process for preparing p-propionolactone comprising adding ketene (CH2=C=O) and formaldehyde in about equimolecular proportions to a solution of triethyl orthophosphate in a solvent selected from the group consisting of acetone, methyl ethyl ketone and ,B-propionolactone,

the concentration of the triethyl orthophosphate being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture, at a temperature of from about to about 20 C.

11. A process for preparing ,B-butyrolactone comprising adding ketene (CH2=C=O) and acetaldehyde in about equimolecular proportions to a solution of at least one catalyst selected from those represented by the following formulas:

wherein R1 represents a member selected from the group consisting of a hydrogen atom, a primary alkyl group of the formula CnH-zn wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, and R2, R3 and R4 each represents a member selected from the group consisting of a primary alkyl group of the formula CnI-Izn+1 wherein n represents a positive integer of from 1 to 5, and an aryl hydrocarbon radical containing from 6 to 10 carbon atoms, in a solvent selected from the group consisting of acetone, ethyl methyl ketone and ,B-propionolactone, at a temperature of from about 10 to about 20C., the concentration of the catalyst being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture.

12. A process for preparing B-butyrolactone comprising adding ketene (CH2=C=O) and acetaldehyde in about equimolecular proportions and R4P Oz to a solution of triethyl orthophosphate in a soivent selected from the group consisting of acetone, methyl ethyl ketone and p-propionolactone, the concentration of the triethyl orthophosphate being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture, at a temperature of from about 10 to about 20 C.

13. A process for preparing p-propionolactone comprising adding formaldehyde and ketene (CH2=C=O) in about equimolecular proportions to a solution of ethyl metaphosphate in a solvent selected from the group consisting of acetone, methyl ethyl ketone and ,B-propionolactone, the concentration of the ethyl metaphosphate being equivalent to from about 0.1 to about 3% by weight of the materials in the reaction mixture at a temperature of from about 10 to about 20 C.

HUGH J. HAGEMEYER, JR.

REFERENCES CITED The following references are of record in the file of this patent:

UNITED STATES PATENTS Number Name Date 2,223,548 Caplan Dec. 3, 1940 2,356,459 King Aug. 22, 1944 OTHER REFERENCES Adler et al., Chem. Ind., 51, 516-21 and 557 (1942).

Certificate of Correction Patent No. 2,450,131. September 28, 1948.

= HUGH J. HAGEMEYER, JR.

It is hereby certified that errors appear in the printed specification of the above numbered patent requiring correction as follows:

Column 6, line 40, Example 4:, for that portion of the formula reading CH C read CH =O'; column 7, line 63, claim 1, for C H read O H column 9, line 33, claim 3, right-hand portion of the formula, for R =?O read R P0 and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Ofiice.

Signed and sealed this 21st day of December, A. D. 1948.

THOMAS F. MURPHY,

Assistant Oommissioner of Patents. 

